Clinical outcomes in COVID-19 patients with cancer who are treated with chemo-or immunotherapy
Journal of Clinical Oncology
; 40(16), 2022.
Article
in English
| EMBASE | ID: covidwho-2009611
ABSTRACT
Background:
Cancer patients infected with COVID-19 are very vulnerable to increased complications and mortality while actively being treated with chemotherapy or immune checkpoint inhibitors (ICIs). The full impact of COVID-19 infections on this subset of patients has not been fully defined. Our goal was to track clinical outcomes in patients with an underlying malignancy and COVID-19 infection who received chemotherapy or ICIs.Methods:
We performed a retrospective chart review of 121 patients (age > 18 years) at the University of Alabama-Birmingham from January 2020 till November 2021 with an advanced solid malignancy that were treated with chemotherapy or ICIs within 12 months of their COVID-19 diagnosis. The aim of this study was to track clinical outcomes including hospitalization rates, ICU admissions, treatments, and deaths of any cause.Results:
A total of 121 patients were examined in this study and 61 received immunotherapy treatment within 12 months. The median age at diagnosis for the ICI group was 62.3 years and 54% were male while for the patients that receive chemotherapy the median age at diagnosis was 65.1 years and 53% were male (Table1). The 3 most common cancers represented in the ICI cohort were lung (30%, NSCLC), liver (13%, HCC) and renal (11%, RCC). While in the chemotherapy group, the 3 most cancers were NSCLC (40%), HCC (12%,), and head & neck (10%, H&N). 25% of patients on ICIs died while only 13% of patients died post chemotherapy. Of the ICI patients that died, 33% were admitted to the intensive care unit (ICU) and 53% received oxygen, steroids and antiviral therapy. For the chemotherapy patients that died, 25% were admitted to the ICU and 50% received oxygen, steroids and antiviral therapy. Patients with lower ECOG (0.98) had lower mortality compared to patients with worse functional status (0.98 vs 1.52;t = 3.20;p < 0.01). Factors associated with increased admission were higher ECOG (1.07 vs 1.67;f = 3.05;p = 0.05), higher AST (21.2 vs 40.9, f = 10.2;p < 0.001), lower absolute lymphocyte count (1122.8 vs 408.9, f = 5.99;p < 0.01) and higher oxygen needs (0.02 vs 1.11, f = 29.5;p < 0.001).Conclusions:
ICI mortality was higher compared to patients receiving chemotherapy, especially for those with reduced functional status. Factors for hospitalization included higher ECOG, higher AST, lower lymphocyte count and increased oxygen needs. However, further investigation still needs to be undertaken to understand if the PD-1-PD-L1 pathway with the subsequent inflammatory cascade post COVID-19 can impact overall survival.
endogenous compound; immune checkpoint inhibitor; oxygen; programmed death 1 ligand 1; programmed death 1 receptor; steroid; absolute lymphocyte count; adult; advanced cancer; aged; Alabama; antiviral therapy; aspartate aminotransferase level; cancer chemotherapy; cancer inhibition; cancer patient; cancer survival; clinical outcome; conference abstract; controlled study; coronavirus disease 2019; diagnosis; drug therapy; female; functional status; hospitalization; human; immunotherapy; intensive care unit; kidney; liver; lymphocytosis; major clinical study; male; medical record review; middle aged; mortality; neck; non small cell lung cancer; outcome assessment; overall survival; retrospective study; signal transduction
Full text:
Available
Collection:
Databases of international organizations
Database:
EMBASE
Type of study:
Prognostic study
Language:
English
Journal:
Journal of Clinical Oncology
Year:
2022
Document Type:
Article
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